Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 16 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 17 |
GO:0110165 | cellular anatomical entity | 1 | 17 |
Related structures:
AlphaFold database: Q4Q0L0
Term | Name | Level | Count |
---|---|---|---|
GO:0038023 | signaling receptor activity | 2 | 4 |
GO:0060089 | molecular transducer activity | 1 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 107 | 111 | PF00656 | 0.700 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.525 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.543 |
CLV_PCSK_PC1ET2_1 | 198 | 200 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 262 | 266 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 339 | 343 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.485 |
DEG_COP1_1 | 159 | 169 | PF00400 | 0.604 |
DEG_ODPH_VHL_1 | 417 | 429 | PF01847 | 0.274 |
DEG_SPOP_SBC_1 | 124 | 128 | PF00917 | 0.652 |
DEG_SPOP_SBC_1 | 77 | 81 | PF00917 | 0.610 |
DOC_CKS1_1 | 145 | 150 | PF01111 | 0.630 |
DOC_CKS1_1 | 174 | 179 | PF01111 | 0.644 |
DOC_MAPK_gen_1 | 13 | 21 | PF00069 | 0.628 |
DOC_MAPK_gen_1 | 400 | 410 | PF00069 | 0.401 |
DOC_MAPK_HePTP_8 | 402 | 414 | PF00069 | 0.430 |
DOC_MAPK_MEF2A_6 | 400 | 408 | PF00069 | 0.438 |
DOC_PP1_RVXF_1 | 344 | 350 | PF00149 | 0.451 |
DOC_PP4_FxxP_1 | 164 | 167 | PF00568 | 0.629 |
DOC_PP4_FxxP_1 | 360 | 363 | PF00568 | 0.362 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 420 | 424 | PF00917 | 0.344 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.226 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.670 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 173 | 178 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.689 |
LIG_14-3-3_CanoR_1 | 13 | 19 | PF00244 | 0.729 |
LIG_14-3-3_CanoR_1 | 138 | 148 | PF00244 | 0.689 |
LIG_14-3-3_CanoR_1 | 199 | 204 | PF00244 | 0.696 |
LIG_14-3-3_CanoR_1 | 218 | 224 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 252 | 258 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 339 | 347 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 403 | 409 | PF00244 | 0.474 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.631 |
LIG_BRCT_BRCA1_1 | 104 | 108 | PF00533 | 0.783 |
LIG_BRCT_BRCA1_1 | 37 | 41 | PF00533 | 0.627 |
LIG_deltaCOP1_diTrp_1 | 468 | 477 | PF00928 | 0.493 |
LIG_eIF4E_1 | 378 | 384 | PF01652 | 0.300 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.640 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.719 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.776 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.479 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.310 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.338 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.338 |
LIG_FHA_1 | 374 | 380 | PF00498 | 0.283 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.373 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.645 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.638 |
LIG_FHA_2 | 160 | 166 | PF00498 | 0.613 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.639 |
LIG_IBAR_NPY_1 | 244 | 246 | PF08397 | 0.496 |
LIG_LIR_Apic_2 | 162 | 167 | PF02991 | 0.631 |
LIG_LIR_Apic_2 | 358 | 363 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 128 | 139 | PF02991 | 0.636 |
LIG_LIR_Gen_1 | 17 | 26 | PF02991 | 0.634 |
LIG_LIR_Gen_1 | 280 | 289 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 38 | 49 | PF02991 | 0.625 |
LIG_LIR_Nem_3 | 128 | 134 | PF02991 | 0.697 |
LIG_LIR_Nem_3 | 17 | 21 | PF02991 | 0.630 |
LIG_LIR_Nem_3 | 249 | 254 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 258 | 264 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 280 | 284 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 326 | 332 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 348 | 352 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 38 | 44 | PF02991 | 0.627 |
LIG_LIR_Nem_3 | 407 | 412 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 74 | 78 | PF02991 | 0.623 |
LIG_NRBOX | 286 | 292 | PF00104 | 0.299 |
LIG_PCNA_yPIPBox_3 | 325 | 339 | PF02747 | 0.300 |
LIG_Pex14_1 | 394 | 398 | PF04695 | 0.300 |
LIG_REV1ctd_RIR_1 | 96 | 105 | PF16727 | 0.633 |
LIG_SH2_CRK | 292 | 296 | PF00017 | 0.262 |
LIG_SH2_STAP1 | 255 | 259 | PF00017 | 0.470 |
LIG_SH2_STAP1 | 292 | 296 | PF00017 | 0.325 |
LIG_SH2_STAT3 | 454 | 457 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.603 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 365 | 368 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 447 | 450 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 454 | 457 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 489 | 492 | PF00017 | 0.360 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.627 |
LIG_SH3_3 | 297 | 303 | PF00018 | 0.219 |
LIG_SH3_3 | 387 | 393 | PF00018 | 0.198 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.723 |
LIG_SH3_3 | 85 | 91 | PF00018 | 0.674 |
LIG_Sin3_3 | 381 | 388 | PF02671 | 0.254 |
LIG_SUMO_SIM_anti_2 | 380 | 387 | PF11976 | 0.333 |
LIG_SUMO_SIM_anti_2 | 423 | 428 | PF11976 | 0.416 |
LIG_SUMO_SIM_par_1 | 380 | 387 | PF11976 | 0.358 |
LIG_TYR_ITIM | 290 | 295 | PF00017 | 0.300 |
LIG_Vh1_VBS_1 | 373 | 391 | PF01044 | 0.215 |
LIG_WRC_WIRS_1 | 278 | 283 | PF05994 | 0.300 |
LIG_WRC_WIRS_1 | 357 | 362 | PF05994 | 0.338 |
LIG_WW_1 | 362 | 365 | PF00397 | 0.300 |
MOD_CDK_SPK_2 | 173 | 178 | PF00069 | 0.650 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.808 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.619 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.597 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.570 |
MOD_CK1_1 | 433 | 439 | PF00069 | 0.314 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.744 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.667 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.691 |
MOD_Cter_Amidation | 196 | 199 | PF01082 | 0.407 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.473 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.590 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.441 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.430 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.366 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.302 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.287 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.451 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.712 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.711 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.687 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.300 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.300 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.257 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.323 |
MOD_N-GLC_1 | 268 | 273 | PF02516 | 0.290 |
MOD_N-GLC_2 | 273 | 275 | PF02516 | 0.201 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.665 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.639 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.387 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.336 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.299 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.322 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.495 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.375 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.377 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.309 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.477 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.364 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.302 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.611 |
MOD_NEK2_2 | 113 | 118 | PF00069 | 0.645 |
MOD_PIKK_1 | 102 | 108 | PF00454 | 0.653 |
MOD_PIKK_1 | 149 | 155 | PF00454 | 0.619 |
MOD_PIKK_1 | 192 | 198 | PF00454 | 0.626 |
MOD_PIKK_1 | 453 | 459 | PF00454 | 0.254 |
MOD_PKA_1 | 199 | 205 | PF00069 | 0.621 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.638 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.627 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.434 |
MOD_Plk_1 | 225 | 231 | PF00069 | 0.627 |
MOD_Plk_1 | 268 | 274 | PF00069 | 0.490 |
MOD_Plk_1 | 35 | 41 | PF00069 | 0.656 |
MOD_Plk_2-3 | 104 | 110 | PF00069 | 0.639 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.551 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.237 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.370 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.346 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.330 |
MOD_Plk_4 | 404 | 410 | PF00069 | 0.474 |
MOD_Plk_4 | 433 | 439 | PF00069 | 0.299 |
MOD_Plk_4 | 491 | 497 | PF00069 | 0.325 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.678 |
MOD_ProDKin_1 | 173 | 179 | PF00069 | 0.704 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.687 |
MOD_SUMO_for_1 | 100 | 103 | PF00179 | 0.631 |
TRG_DiLeu_BaEn_2 | 94 | 100 | PF01217 | 0.655 |
TRG_DiLeu_BaEn_3 | 36 | 42 | PF01217 | 0.600 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.479 |
TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.325 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 365 | 368 | PF00928 | 0.305 |
TRG_ER_diArg_1 | 199 | 201 | PF00400 | 0.668 |
TRG_ER_diArg_1 | 247 | 250 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 402 | 405 | PF00400 | 0.392 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEB9 | Leptomonas seymouri | 50% | 94% |
A0A3S7XBT4 | Leishmania donovani | 37% | 100% |
A0A3S7XBU6 | Leishmania donovani | 89% | 100% |
A0A3S7XC05 | Leishmania donovani | 38% | 100% |
A4HQ64 | Leishmania braziliensis | 68% | 99% |
A4HQ67 | Leishmania braziliensis | 35% | 100% |
A4HQ68 | Leishmania braziliensis | 39% | 100% |
A4IDW4 | Leishmania infantum | 37% | 100% |
A4IDW5 | Leishmania infantum | 88% | 100% |
A4IDW6 | Leishmania infantum | 38% | 100% |
E9ATY5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9ATY6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
E9ATY7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
Q07959 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 93% |
Q4Q0K9 | Leishmania major | 38% | 100% |
Q4Q0L1 | Leishmania major | 38% | 100% |